710-94-1

Basic information

• Product Name: 1,3-DIAZA-SPIRO[4.7]DODECANE-2,4-DIONE
• Synonyms: 1,3-diazaspiro[4.7]dodecane-2,4-quinone
• CAS NO: 710-94-1
• Molecular Formula: C10H16N2O2
• Molecular Weight: 0
• Mol File: 710-94-1.mol
• Article Data: 11

Chemical Properties

• Appearance: /
• Density: 1.17g/cm³
• Refractive Index: 1.534
• CAS DataBase Reference: 1,3-DIAZA-SPIRO[4.7]DODECANE-2,4-DIONE(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-DIAZA-SPIRO[4.7]DODECANE-2,4-DIONE(710-94-1)
• EPA Substance Registry System: 1,3-DIAZA-SPIRO[4.7]DODECANE-2,4-DIONE(710-94-1)

Safety Data

• Hazardous Substances Data: 710-94-1(Hazardous Substances Data)

Usage

Chemical compound

A substance that is commonly used in organic synthesis and medicinal chemistry.

Spirocyclic structure

Consists of a diazabicycloalkane core and a dione functional group.

Pharmaceutical properties

Has been studied for its potential pharmaceutical properties.

Enzyme inhibitor

Ability to act as an enzyme inhibitor.

Antimicrobial activity

Exhibits antimicrobial activity.

Metal catalysts

Has shown promise as a ligand for metal catalysts.

Building block

Serves as a building block for the synthesis of complex organic molecules.

Unique structure

Possesses a unique structure.

Versatile reactivity

Exhibits versatile reactivity.

Valuable tool

Considered a valuable tool for researchers in various fields of chemistry and drug discovery.

InChI:InChI=1/C10H16N2O2/c13-8-10(12-9(14)11-8)6-4-2-1-3-5-7-10/h1-7H2,(H2,11,12,13,14)

Upstream product

• 502-49-8 cycloactanone 
• 151-50-8 potassium cyanide 
• 506-87-6 ammonium carbonate 
• 143-33-9 sodium cyanide 
• 773837-37-9 sodium cyanide 

Downstream Products

• 28248-38-6 1-aminocyclooctane-1-carboxylic acid 
• 92398-65-7 N-(benzyloxycarbonyl)-β-benzyl-L-aspartyl-α-aminocyclooctanecarboxylic acid methyl ester 
• 199330-75-1 1-(tert-butoxycarbonylamino)cyclooctanecarboxylic acid 
• 92398-52-2 methyl 1-aminocyclooctanecarboxylate hydrochloride 
• 16252-65-6 3-amino-1,3-diaza-spiro[4.7]dodecane-2,4-dione 

Relevant articles and documents

Microwave-assisted synthesis of cycloalkanespirohydantoins and piperidinespirohydantoins as precursors of restricted α-amino acids

Cycloalkanespirohydantoins 3 and piperidinespirohydantoins 4 were synthesized from cycloalkanones 9 and piperidones 10 under microwave-assisted conditions. Results are compared with those obtained under thermal conditions. Cycloalkanespirohydantoins 3 were N-protected with Boc group and hydrolyzed under basic conditions to obtain five, six and seven-membered ring restricted α-amino acids 12 in very good overall yields (76-94%). ARKAT USA, Inc.

Synthesis and characterization of novel cycloalkanespiro-5-hydantoin phosphonic acids

A series of new cycloalkanespiro-5-hydantoin phosphonic acids have been synthesized and characterized. The mixture of [(2,4-dioxo-1,3-diazaspiro-alkane- 3-yl)-methyl]phosphonic acids and [(2,4-dioxo-1,3-diazaspiro-alkane-1,3-diyl) dimethyl]diphospho-nic acids was obtained from cycloalkanespiro-5-hydantoins, formaldehyde, and phosphorus trichloride in a molar ratio of 1:2:2, by a procedure modified by us. Their structures were proved by means of IR, 1H, 13C{1H} and 31P NMR spectroscopy. Copyright Taylor & Francis Group, LLC.

HETEROCYCLIC-SUBSTITUTED PIPERDINE COMPOUNDS AND THE USES THEREOF

The invention relates to Heterocyclic-Substituted Piperidine Compounds, compositions comprising an effective amount of a Heterocyclic-Substituted Piperidine Compound and methods to treat or prevent a condition, such as pain, comprising administering to an animal in need thereof an effective amount of a Heterocyclic-Substituted Piperidine Compound